Regarding the addition of bromine to But-2-ene in carbon tetrachloride, correct statement is

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${Br}^{-}$ attacks in the slow step

Product contains two chiral centres

Product is 1, 2 - dibromo butane

Product is a positional isomer of 2, 3 - dibromo butane

answer is C.

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Detailed Solution

$\underset{But - 2 - ene}{{CH}_{3} - CH = CH - {CH}_{3}} \overset{{Br}_{2} / {CCl}_{4}}{\to} \underset{2, 3 - dibromo butane}{{CH}_{3} - \overset{*}{C} H (Br) - \overset{*}{C} H (Br) - {CH}_{3}} {Br}^{+} attacks in the slow step .$

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